Prechel Margaret, Walenga Jeanine M
Assistant Professor, Department of Pathology, Stritch School of Medicine, Loyola University Chicago, Maywood, Illinois, USA.
Semin Thromb Hemost. 2008 Feb;34(1):86-96. doi: 10.1055/s-2008-1066027.
Heparin-induced thrombocytopenia (HIT) is a serious adverse effect of heparin exposure that can progress to severe thrombosis, amputation, or death. HIT is an immune response in which antibodies cause platelet activation, platelet aggregation, the generation of procoagulant platelet microparticles, and activation of leukocytes and endothelial cells. Early diagnosis based on a comprehensive interpretation of clinical and laboratory information is important to improve clinical outcomes. However, limitations of the laboratory assays and atypical clinical presentations can make the diagnosis difficult. Clinical management of patients with HIT is with a non-heparin anticoagulant such as a direct thrombin inhibitor or danaparoid followed by a vitamin K antagonist for long-term treatment. The new anti-factor Xa drugs (fondaparinux, rivaroxaban, apixaban) and other non-heparin antithrombotic agents can potentially be used for the treatment of HIT if clinically validated. Important drug-specific limitations and dosing and monitoring guidelines must be respected for patient safety. Issues still exist regarding the optimal clinical management of HIT.
肝素诱导的血小板减少症(HIT)是肝素暴露的一种严重不良反应,可进展为严重血栓形成、截肢或死亡。HIT是一种免疫反应,其中抗体导致血小板活化、血小板聚集、促凝血血小板微粒的生成以及白细胞和内皮细胞的活化。基于对临床和实验室信息的综合解读进行早期诊断对于改善临床结局很重要。然而,实验室检测的局限性和非典型临床表现可能使诊断变得困难。HIT患者的临床管理是使用非肝素抗凝剂,如直接凝血酶抑制剂或达那肝素,随后使用维生素K拮抗剂进行长期治疗。新型抗Xa因子药物(磺达肝癸钠、利伐沙班、阿哌沙班)和其他非肝素抗血栓药物如果经过临床验证,可能可用于治疗HIT。为了患者安全,必须遵守重要的药物特定局限性以及给药和监测指南。关于HIT的最佳临床管理仍然存在问题。